FDA Recalls Addall XR Shot Liquid Dietary Supplement
ZMB Enterprises is recalling Addall XR Shot liquid dietary supplements because they contain undeclared ingredients 1,4-DMAA, Phenylethylamine, and Phenibut.
The agency’s classification
FDA (Food): Class I
Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 5/5 (Critical).
Highest-severity recall. The hazard can cause serious injury or death. Stop using the product now and follow the agency's instructions.
Our severity reasoning: The source metadata explicitly identifies the agency classification as 'Class I'. According to the severity rubric, an FDA Class I recall corresponds to a score of 5 (Critical).
Plain-English summary
The U.S. Food and Drug Administration (FDA) has issued a Class I recall for Addall XR Shot 1 single bottle, 2 fl. oz., liquid dietary supplements manufactured by ZMB Enterprises. The recall is due to the presence of undeclared ingredients in the product, specifically 1,4-DMAA, Phenylethylamine, and Phenibut.
The affected products were sold between July and December 2025. ZMB Enterprises markets these products online via their website, addallxr.com. The source text does not specify the number of units recalled or the geographic distribution beyond the online sales channel.
Consumers who have purchased this product should stop using it immediately and contact the manufacturer for instructions on how to return the product or obtain a refund. The FDA classifies this as a Class I recall, which is the most serious type of recall, indicating a reasonable probability that the use of or exposure to the violative product will cause serious adverse health consequences or death.
The recalled product
- Product
- Addall XR Shot 1 single bottle, 2 fl. oz., liquid dietary supplement
- Manufacturer
- ZMB Enterprises
- Category
- Food — Dietary Supplement
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Sold between July - December 2025
Distribution
Distribution scope not specified by the agency.
Related recalls
Same hazard · undeclared ingredients
See all →- SevereD'Dioses Mango Ice Pops Recalled for Undeclared Allergens
FDA (Food) · 2026-07-22
- ModerateSuper ProTHIN Plus Dietary Supplement Recalled for Undeclared Dyes
FDA (Food) · 2025-07-02
- LowGaiser's Recalls Ready-to-Eat Bologna Due to Undeclared Meat Ingredients
USDA FSIS · 2025-06-27
- HighFlour tortillas recalled due to undeclared wheat allergen
FDA (Food) · 2024-05-29
- ModerateMilk N Cookies Keto Brick recalled for undeclared MCT oil and acacia fiber
FDA (Food) · 2024-02-07
Similar recalls
- CriticalUltra ZX Dietary Supplement Recalled for Undeclared Sibutramine and Phenolphthalein
FDA (Drugs) · 2015-05-13
- SevereZero Xtreme Dietary Supplement Recalled for Undeclared Sibutramine
FDA (Drugs) · 2018-11-21
- CriticalFossil Fuel Products Recalls RezzRX Capsules for Undeclared Ingredients
FDA (Drugs) · 2014-04-30
- CriticalBethel 30 capsules recalled for undeclared active ingredients
FDA (Drugs) · 2013-09-04
- CriticalFDA Recalls Silver Bullet Male Enhancement Capsules for Undeclared Active Ingredient
FDA (Drugs) · 2020-01-08
- CriticalFDA Recalls ZRECT for Women Herbal Supplement Due to Undeclared Drugs
FDA (Drugs) · 2017-07-19